DE977979C - - Google Patents
Info
- Publication number
- DE977979C DE977979C DE1963977979 DE977979A DE977979C DE 977979 C DE977979 C DE 977979C DE 1963977979 DE1963977979 DE 1963977979 DE 977979 A DE977979 A DE 977979A DE 977979 C DE977979 C DE 977979C
- Authority
- DE
- Germany
- Prior art keywords
- binder
- polyurethane
- diols
- glycol
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000011230 binding agent Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 239000004449 solid propellant Substances 0.000 claims description 8
- 239000003380 propellant Substances 0.000 claims description 7
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 6
- HDIFHQMREAYYJW-XGXNLDPDSA-N Glyceryl Ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(O)CO HDIFHQMREAYYJW-XGXNLDPDSA-N 0.000 claims description 6
- 239000004014 plasticizer Substances 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims description 3
- -1 polypropylene- Polymers 0.000 claims description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 2
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims description 2
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 claims description 2
- 235000010445 lecithin Nutrition 0.000 claims description 2
- 239000000787 lecithin Substances 0.000 claims description 2
- 229940067606 lecithin Drugs 0.000 claims description 2
- 229920001451 polypropylene glycol Polymers 0.000 claims description 2
- 239000011833 salt mixture Substances 0.000 claims description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 2
- 150000002009 diols Chemical class 0.000 claims 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 4
- 229920002635 polyurethane Polymers 0.000 claims 4
- 239000004814 polyurethane Substances 0.000 claims 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- 239000000654 additive Substances 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 229920005749 polyurethane resin Polymers 0.000 claims 3
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims 2
- 238000007792 addition Methods 0.000 claims 2
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 claims 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- 229910052742 iron Inorganic materials 0.000 claims 2
- 239000012948 isocyanate Substances 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- 229920005989 resin Polymers 0.000 claims 2
- 239000011347 resin Substances 0.000 claims 2
- HDIFHQMREAYYJW-FMIVXFBMSA-N 2,3-dihydroxypropyl (e)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C\CCCCCCCC(=O)OCC(O)CO HDIFHQMREAYYJW-FMIVXFBMSA-N 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 238000005266 casting Methods 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 claims 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims 1
- 239000000446 fuel Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 238000004898 kneading Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229920003002 synthetic resin Polymers 0.000 claims 1
- 239000000057 synthetic resin Substances 0.000 claims 1
- 150000004072 triols Chemical class 0.000 claims 1
- CJJXHKDWGQADHB-DPMBMXLASA-N (z,12r)-12-hydroxyoctadec-9-enoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O CJJXHKDWGQADHB-DPMBMXLASA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6629—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/222—Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Description
Polypropylenglycol 41,90·/»Polypropylene glycol 41.90 · / »
Toluylendiisocyanat 22,35%Toluene diisocyanate 22.35%
Weichmacher auf der Basis Glycerin-MonoricinoleatPlasticizer based on glycerine monoricinoleate
(Flexricin) 10,15°/·(Flexricin) 10.15 ° /
Butylenglycol 5,60%Butylene glycol 5.60%
Dioctylsebacat 20,00%Dioctyl sebacate 20.00%
18,5% dieses Binders werden mit einer Oxydationssalzmischung, bestehend aus18.5% of this binder is mixed with an oxidation salt mixture, consisting of
Ammoniumperchlorat 80,25%Ammonium perchlorate 80.25%
Ferrocen 1,00%Ferrocene 1.00%
Lecithin 0,25%Lecithin 0.25%
— wie oben beschrieben — verarbeitet- as described above - processed
Die fertigen Treibsätze hatten eine Zugfestigkeit von 11 kg/cm2 und eine Dehnung von 28%.The finished propellants had a tensile strength of 11 kg / cm 2 and an elongation of 28%.
In der folgenden Tabelle werden einige weitere Bindemittelmischungen angegeben, wie sie zur Verar- ao beitung bei Feststofftreibsätzen gemäß der Erfindung besonders vorteilhaft sind.In the following table some further binder mixtures are given, as they are for processing ao Processing in solid propellants according to the invention are particularly advantageous.
(Vt)(Vt)
(V.)(V.)
<·/·)<· / ·)
Glycerinmonoricinoleat
(Flexricin)
2-Hydroxymethyl-4-
oxy-pentanol-1
Butylenglycol
Dioctylsebacat
Toluylendiisocyauat ..Desmophs
Glycerol monoricin oleate
(Flexricin)
2-hydroxymethyl-4-
oxy-pentanol-1
Butylene glycol
Dioctyl sebacate
Toluene diisocyanate.
9,46
6,94
19,97
24,5739.06
9.46
6.94
19.97
24.57
3,67
3,15
19,95
20,7852.45
3.67
3.15
19.95
20.78
10,15
5,60
20,00
22,3541.90
10.15
5.60
20.00
22.35
Zugfestigkeit, kg/cm2 ..
Dehnung, % Ferrocene
Tensile strength, kg / cm 2 ..
Strain, %
3,00
22
160100.00
3.00
22nd
160
2,00
20
100100.00
2.00
20th
100
2,00
14
130100.00
2.00
14th
130
Claims (15)
Zugfestigkeit, Dehnung und Elastizität, verleihen,mechanical properties, in particular with regard to individual ones, explained in more detail:
Tensile strength, elongation and elasticity, impart,
die Abbindezeit, innerhalb der die Erhärtung ein- 3»on the other hand, in the production of the propellant, Example 1
the setting time within which the hardening 3 »
Feststofftreibsätze Polyurethane zu verwenden, jedochIt has already been proposed as a binder for component manufactured.
Solid propellants use polyurethanes, however
lendiamin) oder einem kurzkettigen Diol, z. B. Butylenglykol oder einem Amin. Ammoniumperchlorat 80,25 Vosuch as a triol (hexanetriol, glycerol monoricinoleate, 19% of this binding mixture then becomes 2-hydroxy-methyl-4-oxy-pentanol-1) and / or an oxidation salt mixture of the following square (NN, N'N'- tetrakis ^ -hydroxy-propyl-ethy-45 composition added,
lenediamine) or a short-chain diol, e.g. B. butylene glycol or an amine. Ammonium perchlorate 80.25 vol
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1963977979 DE977979C (en) | 1963-10-10 | 1963-10-10 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1963977979 DE977979C (en) | 1963-10-10 | 1963-10-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE977979C true DE977979C (en) | 1974-08-08 |
Family
ID=5646467
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE1963977979 Expired DE977979C (en) | 1963-10-10 | 1963-10-10 |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE977979C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5091439A (en) * | 1986-06-17 | 1992-02-25 | Ciba-Geigy Corporation | Process for curing polyurethane coatings and compositions |
-
1963
- 1963-10-10 DE DE1963977979 patent/DE977979C/de not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5091439A (en) * | 1986-06-17 | 1992-02-25 | Ciba-Geigy Corporation | Process for curing polyurethane coatings and compositions |
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